Metadata | |
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ID | DOID:0060781 |
Name | congenital secretory sodium diarrhea 3 |
Definition | A secretory diarrhea that has_material_basis_in homozygous or compound heterozygous mutation in the SPINT2 gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/19185281 |
Xrefs | |
Subsets |
DO_rare_slim |
Synonyms |
congenital secretory sodium diarrhea 3 syndromic [EXACT] congenital secretory sodium diarrhea 3 with or without other congenital anomalies [EXACT] congenital secretory sodium diarrhoea 3 [EXACT] congenital secretory sodium diarrhoea 3 syndromic [EXACT] congenital secretory sodium diarrhoea 3 with or without other congenital anomalies [EXACT] |
Parent Relationships |
is_a physical disorder is_a autosomal recessive disease is_a secretory diarrhea |